α-GLOBIN GENE ORGANISATION AND PRENATAL DIAGNOSIS OF α-THALASSAEMIA IN CHINESE-Reference-Cited by-同舟云学术

α-GLOBIN GENE ORGANISATION AND PRENATAL DIAGNOSIS OF α-THALASSAEMIA IN CHINESE

Published:1985-02 Issue:8424 Volume:325 Page:304-307
ISSN:0140-6736
Container-title:The Lancet
language:en
Short-container-title:The Lancet

Author:

Zeng Y.-T.,Huang S.-Z.

Publisher

Elsevier BV

Subject

General Medicine

Reference12 articles.

1. A survey of hemoglobinopathy in 600,000 people of 20 provinces, cities and autonomous regions of China;National Coordination Group of Hemoglobinopathy Research;Natl Med J China,1983

2. Two different molecular organizations account for the single α-globin gene of the α-thalassemia-2 genotype;Embury;J Clin Invest,1980

3. Prenatal diagnosis of hemoglobinopathies;Kan;Ann NY Acad Sci,1980

4. Application of endonuclease mapping to the analysis and prenatal diagnosis of thalassemia caused by globin-gene deletion;Orkin;N Engl J Med,1978

5. First- trimester fetal diagnosis for haemoglobinopathies: three cases;Old;Lancet,1982

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